A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249683



Internal ID20816723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51980122..51981040hg38UCSC Ensembl
chr1:52445794..52446712hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547900
Supporting Variants
Samples
Known GenesRAB3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249683
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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